Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11934458-11934798 | Common:6; Rare:105; Clinvar:6; Clinvar (benign):1 | ||||
chr1:11980066-11980338 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11980366-11980537 | Common:2; Rare:53; Clinvar (benign):5 | ||||
chr1:12019181-12019625 | Common:5; Rare:158 | ||||
chr1:12063144-12063445 | Common:2; Rare:51 | ||||
chr1:12063856-12064084 | Common:1; Rare:44 | ||||
chr1:12166818-12167052 | Common:3; Rare:68 | ||||
chr1:12344585-12344865 | Rare:39 | ||||
chr1:13699761-13699993 | Rare:47 | ||||
chr1:13699995-13700368 | Common:2; Rare:94 | ||||
chr1:13700563-13700868 | Rare:75 | ||||
chr1:13730759-13731402 | Common:3; Rare:148 | ||||
chr1:13749068-13749583 | Common:2; Rare:184 | ||||
chr1:13749752-13749802 | Rare:11 | ||||
chr1:15153604-15153797 | Common:2; Rare:53 |